亚洲中文字幕特级毛片-亚洲制服丝袜中文字幕-亚洲制服丝袜在线观看-亚洲制服欧美自拍另类-免费一级黄色-免费一级国产生活片

掃碼關注公眾號           掃碼咨詢技術支持           掃碼咨詢技術服務
  
客服熱線:400-901-9800  客服QQ:4009019800  技術答疑  技術支持  質量反饋  人才招聘  關于我們  聯系我們
欧美变态口味重另类在线视频,夜夜爱夜夜做夜夜爽,风流老熟女一区二区三区
首頁 > 產品中心 > 標記一抗 > 產品信息
Rabbit Anti-MYH7B/Cy3 Conjugated antibody (bs-9862R-Cy3)
訂購熱線:400-901-9800
訂購郵箱:sales@www.chomd.com.cn
訂購QQ:  400-901-9800
技術支持:techsupport@www.chomd.com.cn
說 明 書: 100ul  
100ul/2980.00元
大包裝/詢價
產品編號 bs-9862R-Cy3
英文名稱1 Rabbit Anti-MYH7B/Cy3 Conjugated antibody
中文名稱 Cy3標記的肌球蛋白重鏈7抗體
別    名 adult 1; Beta myosin heavy chain; cardiac muscle beta isoform; CMD1S; CMH1; MPD1; MYH1; MYH1_HUMAN; MYH7; MYH7_HUMAN; Myhc slow; MyHC-2x; MyHC-beta; MyHC-IIx/d; MyHC-slow; MYHCB; Myopathy, distal 1; Myosin heavy chain (AA 1-96); Myosin heavy chain 1; Myosin heavy chain 2x; Myosin heavy chain 7; Myosin heavy chain; Myosin heavy chain IIx/d; Myosin heavy chain slow isoform; Myosin heavy chain, cardiac muscle beta isoform; Myosin, heavy chain 7, cardiac muscle, beta; Myosin, heavy polypeptide 7, cardiac muscle, beta; Myosin-1; Myosin-7; Rhabdomyosarcoma antigen MU RMS 40.7A; skeletal muscle; SPMD.  
規格價格 100ul/2980元 購買        大包裝/詢價
說 明 書 100ul  
研究領域 心血管  發育生物學  信號轉導  干細胞  細胞骨架  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應 (predicted: Human, Mouse, Rat, Chicken, Horse, )
產品應用 IF=1:50-200 
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
分 子 量 213kDa
性    狀 Lyophilized or Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human MYH7
亞    型 IgG
純化方法 affinity purified by Protein A
儲 存 液 0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.
保存條件 Store at -20 °C for one year. Avoid repeated freeze/thaw cycles. The lyophilized antibody is stable at room temperature for at least one month and for greater than a year when kept at -20°C. When reconstituted in sterile pH 7.4 0.01M PBS or diluent of antibody the antibody is stable for at least two weeks at 2-4 °C.
產品介紹 background:
Myosin heavy chains are ubiquitous Actin-based motor proteins that convert the chemical energy derived from ATP hydrolysis into the mechanical energy that drives diverse motile processes in eukaryotic cells, including cytokinesis, vesicular transport and cellular locomotion. Muscle myosin is a heterohexamer consisting of two myosin heavy chains and two associated nonidentical pairs of myosin light chains. The seven myosin heavy chain isoforms that predominate in mammalian skeletal muscles include two developmental isoforms, MHC-embryonic (MYH3) and MHC-perinatal (MYH8); three adult skeletal muscle isoforms, MHC IIa (MYH2), MHC IIb (MYH4) and MHC IIx/d (MYH1); and MHC-∫/slow (MYH7 or MHC-∫), which is also expressed in cardiac muscle. Research indicates that mutations of the MYH7 gene causes hypertrophic cardiomyopathy.

Function:
Muscle contraction.

Subunit:
Muscle myosin is a hexameric protein that consists of 2 heavy chain subunits (MHC), 2 alkali light chain subunits (MLC) and 2 regulatory light chain subunits (MLC-2).

Subcellular Location:
Cytoplasm, myofibril. Note=Thick filaments of the myofibrils.

DISEASE:
Defects in MYH7 are the cause of cardiomyopathy familial hypertrophic type 1 (CMH1) [MIM:192600]. Familial hypertrophic cardiomyopathy is a hereditary heart disorder characterized by ventricular hypertrophy, which is usually asymmetric and often involves the interventricular septum. The symptoms include dyspnea, syncope, collapse, palpitations, and chest pain. They can be readily provoked by exercise. The disorder has inter- and intrafamilial variability ranging from benign to malignant forms with high risk of cardiac failure and sudden cardiac death.
Defects in MYH7 are the cause of myopathy myosin storage (MYOMS) [MIM:608358]. In this disorder, muscle biopsy shows type 1 fiber predominance and increased interstitial fat and connective tissue. Inclusion bodies consisting of the beta cardiac myosin heavy chain are present in the majority of type 1 fibers, but not in type 2 fibers.


Similarity:
Contains 1 IQ domain.
Contains 1 myosin head-like domain.

Database links:

Entrez Gene: 58498 Human

Omim: 612147 Human

SwissProt: Q01449 Human

Unigene: 75636 Human



Important Note:
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
版權所有 2004-2026 www.www.chomd.com.cn 北京博奧森生物技術有限公司
通過國際質量管理體系ISO 9001:2015 GB/T 19001-2016    證書編號: 00124Q34771R2M/1100
通過國際醫療器械-質量管理體系ISO 13485:2016 GB/T 42061-2022    證書編號: CQC24QY10047R0M/1100
京ICP備05066980號-1         京公網安備110107000727號
主站蜘蛛池模板: 一卡二卡三卡四结衣| 国产波霸爆乳一区二区-亚 | 亚洲成AV人片在线观看无码18| 亚洲欧洲另类春色校园小说,欧美人成片免费 | 中文字幕无线码一区非州| 亚洲精品91在线精品探花在线 | 亚洲精品网站??在线播放glf | 久久国乱精品| 51国产黑色丝袜高跟鞋美女| 亚洲国产一二三精品无码绿巨人西野翔| 男女猛进猛出激情四射| 国产乱码一区二区三区四区AV | 黑人啊灬啊灬啊灬快灬深的意思老外做爱一绿片| 国产摄像头无码Av | 城中村工棚嫖妓v88AV| 亚洲黄色在线观看网站黄色| 精品人妻中文字幕一区二区三区蜜桃| 91精品国产色综合久久不卡98口| 性人久久久sm| 丰满少妇人妻无码精品内射 | 国产成人精品电影在线观看81| 一本久久伊人热热精品中文精品伊人久久久99热这里只 | 亚精区区一区区二在线观看区区一区区二在线观看| 女人又爽 又黄 免费视频| 国产XXX?做受性欧关88| 午夜精品深夜一区二区91草莓| 国偷精品无码久久久久蜜桃软件| 亚洲综合图色婷婷| 精品国产va久久久久久久冰软件| 羽月希人妻初乳DASD510| 久久久综合香蕉尹人综合网演员表| 7777精品久久久大香线蕉小说474 7777精品伊人久久久大香线蕉超级流畅 | 岛国无码免费视频网此导航| 亚洲精品高清国产久久久久久| 狠狠色婷婷久久一区二区四季AV| 亚洲人成无码网站玖玖99热国产 | 亚洲熟女乱综合一区二区三区8P| 精品久久久久久无码人妻热,国产成A| 亚洲尤物一区二区21页| 国产在线精彩视频二区_国产91| 亚洲乱码少妇99P-=三四区|